I am curious and wondering how many people with hypothyroidism had their tonsils out when they were younger. I had mine out at 13 because I kept getting strep throat. I am reasoning how near the tonsils are to the thyroid and could there be a correlation.
I am curious and wondering...: I am curious and... - Thyroid UK
I am curious and wondering...
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Katherine1234
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helvellaAdministrator
I had tonsillitis quite regularly until I was about 13 - when it just stopped. I still have my tonsils all these decades later.
My mother was never convinced that I should have mine out. But my older sister had tonsils and adenoids out. Did that make her re-think? I don't know.
It happened to my eldest son too helvella. I decided not to have his removed. He still suffers on and off with sore throats. I am of the believe that nature did not put anything there that was not needed. I am hanging on to my gallbladder at present like crazy. Even though they want to take it out. I was just wondering as thyroid is so near to tonsils. Also I was reading there is a connection with tonsils and gallbladder.
Been wondering this for a long time. I had mine out when I was about 4 years old.
Here's an article that might interest you:
organiclifestylemagazine.co...
Thank you greygoose, I will have a read.
An interesting read greygoose. I am of the belief that nature would not have put anything there if it did not serve a purpose.
Exactly! I totally agree.
My son, had terrible problems with his tonsils when he was about 3. Doctors did nothing to help - told me to give him ice cream when he couldn't even swallow a sip of water without vomiting. I did my own research - which wasn't easy 50+ years ago - and came to the conclusion that vit C was the answer. And it was! Not that that was easy, either! Had to buy it in a pharmacy and the pharmacists didn't want to sell it to me, kept asking me why I wanted it. I kept telling them to mind their own B business and hand over the goods! Damned cheek. 
But, his tonsils pretty soon cleared up and he's had no health problems to speak of in the past 50+ years.
Yes indeed large doses of vitamin C every 2 hours to bowel tolerance would take out an infection of the tonsils. Well done you
Thank you. Vit C is wonderful stuff!
I had tonsilitus time and time again as a young child. But my GP fought for me not to have my tonsils out. I still have them. I grew out of the bugs. I was an only child. Sending me to school was like throwing me into a germ factory totally unprotected.
I would have rather had kept mine.
Well ffs one more thing to think about in retrospect… if we knew then what we know now.
I had my adenoids out when I was 5.
Reading about this just makes me sad.
I had mine out when I was around 7 or 8. Mine were very enlarged, not infected and I had adenoids removed. This was in the 70's where it seems anything not essential for life was whipped out.
Mine were very enlarged Sparkingsunshine but I kept getting strep throats age 11 to 13, so they took them out. I realise I was quite old to have them out. Horrible operation.
I had strep throat over and over and over again and goodness knows how many anti-biotics my mother was dead against removal but FINALLY had my tonsils out aged 19! Strangely Mum was a Vit C convert but only used it for colds - if only she had tried it for the throat! I am certain the anti-biotics weren't good for me. I don't do very well with lots of pharmaceutical stuff hence I self treat on NDT.
Yes, I was aged 4 when my tonsils were removed but I continued to have a number of low level health issues during my formitive years which doctors generally dismissed!
I knew something was far wrong but medics had no ideas so I had to start researching myself from a very low knowledge base!!
Fast forward to 2017 when after a series of debilitating health issues and much research it turned out that I have a form of Thyroid Hormone Resistance and need high dose T3-only
I suspect at that early age my T3 level was already low and my tonsil related problems were an early sign of what was to come
I have read of this link in the past but my erratic filing system has since resulted in the lost the details....must try and retrace those early steps.
Thyroid hormones, particularly T3 as the active hormone, are key to the function of most, if not all, parts of the body
The only thing I remember about that early hospital stay is the ice cream....but I suspect it was more significant than just a bowl of refreshing ice cream
So yes, I'm convinced there is a correlation.
I am on T3 now DippyDame, I was on a 100mcg of T4, 5 years later I was way over on a blood test, Endo reduced T4 and added T3. I am now 75mch T4 and 20 mcg T3. Doing slightly better not that magic bullet I was hoping for.
Perhaps your dose still isn't right for you.
Your previously high FT4 suggests you have impaired T4 to T3 conversion
Did you have low FT3 reading with that high FT4...a sign of poor T4 to T3 conversion....and the need for added T3
is that why your endo introducec T3?
The fact that you felt " slightly better" after adding T3 suggests to me that you still need more T3
Suggest you ask to trial a further T3 increase ....some of us just need more. This is to ensure enough T3 reaches the nuclei of the cells where it attaches to the T3 receptors and becomes active....until that point T3 remains inactive
We are all different with different needs...not necessarily what a textbook indicztes
The chances are that the tonsilitis is a symptom of T3 undermedication...at whatever age
i don't think removing the tonsils is the answer it didn't stop me having a lot of health issues throughout life...and I'm aged 79!!
I need appropriatre thyroid medication....
I need 100mcg T3 only!
Yes, low T3 it just scraped in but t4 was off the charts. Endo has upped my dose to 30mcg instead of 20, but I was too scared to take it. I have another blood test booked in January, I will see then. My TSH is now suppressed my T4 was 18 last time and my T3 5.1
Please don't be scared of T3. If another 10 is too much, you'll feel it and can tweak it down.
Good, a clued up endo....hopefully!
I would use the extra T3 to gradually increase your dose
You definitely need more!
Instead of jumping straight to 30 mcg I would cut the extra tablet (10mcg?) into four× 2.5mcg and add 1 quarter to your 20mcg dose, wait 2 weeks, add the next piece and repeat until you reach the 30mcg dose then see how you feel...note any symptoms
Do you keep a diary of your thyroid journey noting medication symptoms test results etc....I found this invaluable
Don't be scared of T3 it's your way to better health....but ensure that you add any increase gradually to allow your body to slowly adjust to having more hormone
You will soon know if it's too much....just drop the dose a little!
I've taken up to 212.5 mcg T3 as I was titrating my dose up....that became too much despite my having a form of Thyroid Hormone Resistance, which I don't think you have
As my T3 receptors adjusted with the dose I settled on 100mcg.
The late T3 expert Dr John Lowe whose work I followed took around 150mcg daily for most of his adult....he died as the result of a traffic accident .....nothing to do with T3!!
"The book he wrote with Dr. Gina Honeyman-Lowe, Your Guide to Metabolic Health (2003), describes when T3 should be trialed, how to go about it, and complementary supplements and methods to monitor progress. Many patients start on a “full replacement dose” of pure T3 (i.e. the amount a normal thyroid gland would produce per day: 20 – 30 mcg), but the starting dose depends on the patient’s health status, severity of symptoms, and other factors. Dr Lowe generally prescribed a single daily dose of pure T3 to be increased gradually by 12.5 – 25 mcg at 1 – 2 week intervals, and then more modest increases of 6.25 mcg as the patient appears to approach the “therapeutic window” (Lowe, 2008) – i.e. “a dose at which the patient has no symptoms of overstimulation, and hypothyroid-like symptoms improve or disappear altogether.”
Their methods are also described in the following e-book which is available on Amazon for £3.56 or free if you have Amazon Prime. It is called "Impaired Sensitivity to Thyroid Hormone (Thyroid Hormone Resistance)" by Hugh A Hamilton
I recommend it!
The journey might be a tad bumpy but 30mcg is nothing to be afraid off. There are far too many scaremongering stories about T3. It just needs to be treated with respect and to be increased slowly!
The more you learn the more comfortable with it you will become!
Don't give up!!
I had my tonsils and adenoids out when I was 10.
I had been developing tonsillitis over and over again, which always ended up with me getting a high fever and being prescribed antibiotics.
My GP at the time had a simple rule. Have tonsillitis three times in a year and the patient would be allowed to keep their tonsils and adenoids. Have tonsillitis four times in a year and they got removed.
I never regretted getting mine removed because life was so much more pleasant without getting painfully ill over and over again.
I had terrible tonsillitis growing up, was put on the waiting list for removal at age 16, turned 18 (almost 30 years ago)& hadn't had it for a year so I didn't bother. Only had it once or twice as a adult.
I had tonsillitis a lot as a child and teen, but our family doctor was against removing them. Both of my children suffered with a lot of strep as kids and even as young adults, and I often caught it from them as an adult.
Not for me, I didn't suffer with sore throat until I became an adult. I've often that joked I have an overactive immune system. It was only when my poor thyroid couldn't hold off the autoimmune attack that I suffered with infections, and still do when undertreated.
Never knowingly had tonsillitis, and im nearer 60.
Wow! you lucky bunny I had it all and the yellow dots on my tonsils
Wonder if its hereditary. None of my daughters were prone.
I am not to sure that I buy into the hereditary gene theory 66olives.
don’t have tonsillitis and didn’t have mine out either!
My son’s repeat tonsillitis and ear infections stopped immediately when - aged 2 - I reduced the quantities of dairy he took in. He never had another ear infection.
But had been on the cusp of having grommets before I changed his diet.
Katherine1234,
Yes, awfully sickly child so tonsils and adenoids removed aged 10.
Appendix removed aged 12.
Then awfully sickly teenager lasting into early twenties with swollen lymph nodes, constantly testing negative for glandular fever and brucellosis. Looking back I think this was the early ravages of emerging Hashimotos.
I’ve read some research looking at the consequences of removing any lymphatic tissue and later autoimmunity is one suggestion.
radd. I will still have swollen lymph nodes, they are never down. I have been diagnosed with ME/CFS which I think is just a catch all diagnosis. I test positive for epstein barr.
I had my appendix out at 36, I was a late developer lol. Mine was on the verge of bursting so had no choice and was found to be gangrenous. I got hypo around 15 years later.
yes I had my tonsils out aged 8 but so did many of my contemporaries in the 1950s.
yes awful time as a child every winter tonsillitis and sinus infections- finally had tonsils removed at 13! Still had sinus issues and still do!!
I was 13 Robinface. I hear that is late to have them out.
I had mine. Out when I was a child
I have never had tonsillitis but I grew up with asthma and recently diagnosed severe. I had more sinus problems and one side of my nose quarterised at about 13, due to bouts of chest infections
I had my adenoids out aged 5 but my tonsils stayed, even though I kept getting tonsillitis. I eventually grew out of so many bouts of it.
I too had my tonsils and adenoids removed at about 7 /8 years old. We, my younger brother & I were always having bugs from school.
It was the done thing in those days late 1950s at our age to have your T& A removed.!
Yes I remember the horrible purple drink I had to down in one!! Covalence reward was jellies with some Ice cream …..sore throat foods!
I’m now on a trial of T3/T4……
I am now on a T3/T4 trial Tea7light
Tonsils, adenoids and a sinus washout emergency surgery at GOSH when two and a half. Sore throats and etc continued with being absolutely poleaxed twice a year, normally around October and March, when I would be delerious (sp) for 48 hours and take a week to recover. Last one of those was about 30 years ago when my son was about 3. Has a sinus washout and widening about 20 years ago. A mixture of T3 and moving out of a vale finally got rid of it but a couple of months ago OH brought me a big back from France and I’ve had mucous problems again. I get a mild sore throat and left earache when I’m tired. I’m deaf with a mainly profound loss in my left ear.
Sounds like me from the ages of 7 to 26 when Graves kicked in. I then seemed to get it now and again, but at the first sign I suck Strepsils and mostly that seems to ward it off. It is very rare for me the last few years since a good level of Vitamin D. Never had my tonsils out, but they are in such a state, I wonder if they are doing any good!
I had my tonsils out when I was 8 years old, but I had tonsillitis at least 3-4 times a year when I was younger that required antibiotics, so it was good that they were removed.
I can even remember the ward I was in with the other children, and we got really lovely pistachio ice cream for cooling the throat! Silver lining ... 😉
I think most people in my age group will have had tonsils out. It was very rare at school to find anyone who still had tonsils by the time they were at the end of primary school.
That is amazing and there was then a big back turn in the 80's and doctors were told not to remove them. They never told us the reason why.
has to be cost!
I had my tonsils out when I was 4. I don’t remember being ill having tonsillitis or similar but guess I must have. My mum was a nurse so I’m sure she must have considered it carefully prior to agreeing. did have & still do have Asthma. As others have said it was common in the 50’s.
Yes I had mine out. I think Dr P used to think there was a link.
Thank you mstp, I will have a look and see if I can find more information from him.
He passed away last year but his book might say something about it.
I had mine out before I was 12 in the fifties because I was frequently ill with bad colds. I remember nearly every Christmas I was sick in bed, which really got my mother down. Anyway, my health did not improve and I continued to suffer until I was in my twenties. I had moved away from home and my GP said he thought I had a sinus infection (chronic) and sent me to a specialist who said I had a defected septum. I was continually blowing my nose, producing black stuff (to me that was normal). Anyway, the specialist performed surgery on my nose, and I would say that normalised me! So tonsils could have been left alone; I caught a cold in the hospital anyway due to them leaving a window open above my bed, and so I wasn't able to go home at the same time as all the other kids who had it done.
That was a lifetime away. I'm 80 now and not suffering like I did as a child/young person.
i had no issues with tonsillitis as a kid , so i have my own tonsils still, didn't stop me becoming autoimmune hypo in my 30's though .
my daughter had regular horrible bouts of tonsillitis (2 or 3 a year) from about age 12 on wards.... she didn't quite reach the threshold for removing them , but i would not have been keen to allow it even if she did ... due to vague idea's along the lines of 'if they are the first line of defence, and you remove , what gets attacked instead ? "
she is now 26 and hasn't had a bout of tonsilitis for several yrs now , so i think she's grown out of it ....
mind you her tonsils are not pretty anymore ... full of massive craters.
I agree with you tattybogle. They are our first line of defence and makes a lot of our fighter T cells too.
Believe I was misdiagnosed with hypothyroidism and I still have my tonsils
silverbelle what do you mean misdiagnosed with hypothyroidism, have they said you are hypothyroid?
I had no sx back in 2012 when I had an annual exam and labs. Dx on a single TSH and blindly started Levo and I stared to develop hyperthyroid sx and when I complained I was told I just didn't recall what it felt like to feel "healthy" . I had been walking 2 miles 2x a week working on rehabing from a medial meniscus surgery and within a few months I was less and less able . I was on Levo 1/2013 to 7/2017 when I decided to wean myself off Levo and yes I did tell the doctor. I had to because I had become a cripple and had developed low grade hypertension and placed on a combo of 2 drugs when previous my BP was always on the low side, but I had great energy and felt well. I am not as well as I was 12/2012, but I have been able to shake off most of the symptoms I developed and in 2017 -2018 I also weaned myself off the 2 drugs. I have no doubt it all started with Levo, but I do have acute joint issues! Thank You for asking .
What a crazy journey silverbelle. I am not so sure most doctors know what they are doing with thyroid. Have you tried MSM natural sulphur for your joints? It got rid of my joint pain and even the pain of a frozen shoulder! It gives you lots of energy and the tummy likes it too.
I have tried MSM, but no real results is there a brand or name you would recommend. I generally buy on Amazon cause things are so hard to source here in the USA, but if there is something you like I just might try and find it and give it a try. Thank You
Back in the early fifties I had recurring tonsillitis - I remember the doc painting my tonsils but I can’t remember or never knew what he ‘painted’ them with but it did the trick as I still have them !
I bet it was old fashion iodine. That stuff kills anything. I am started to think that doctors knew a lot more back in the old days.
Had mine out when I was ten, my Mother was firmly of the mind that the Doctor knows best!
Yes, I've wondered about this too - I had my tonsils removed aged 16 & looking back, I think my thyroid problems started after that.
Geeze! that was late jillyana, I thought me having them out at 13 was late. I never felt right after the removal of my tonsils.
I ended up with hashi's & wonder if it was linked
I don't have hashi's I am normal underactive thyroid. Although I wish I had known then what I know now, I would have treated it with iodine, retinol vitamin A, beef liver capsules, selenium and L tyrosine.
I had mine out when I was 16. I couldn’t even lift my head off the pillow I was that ill when I had tonsillitis! So now, if I ever get a really sore throat, I KNOW I am going to be REALLY ill, and I usually am. Personally speaking, having my tonsils out was the best thing that could have happened to me at the time as it has saved me from a lot of suffering in my adult life.
how awful, I know that pain well and not being able to lift my head of the pillow, so dehydrated too, swallowing water was so painful.
Still got my tonsils. Adenoids gone as a young lad and I got the ice cream still afterwards to the annoyance of my 2 older brothers who had tonsils out. They do not have thyroid issues.
I had glandular fever around 18 and I wonder about effects of that. 25 years later to finding thyroid issue though.
I had glandular fever a6 16 Sleepman. And last year I had it reactivated. My son had glandular fever at 18. There is a link with glandular fever and thyroid.
Mum is same as me so I think mine is genetic weekness ... gluten and thyroid , low conversion
- perhaps glandular fever has a role in triggering though - I had read something
I think Mum has a bad fever at the start of her troubles.
I am wanting my kids to get TSH/T3 and T4 normal levels and check TPO and TGA in case they ever do get it they have a baseline normal level.
I was 6 years old when I had my tonsils and adenoids removed after repeated ear infections with perforated eardrums. I had one ear infection afterwards and that was it.
There was a ‘craze’ of taking tonsils out when I was a child in the 1960s. One school year I think I was off sick more often than I was in, because each time I went back I got tonsillitis again! My Mum was very reluctant to get them taken out, and in the end the doctor said if I got it one more time he was going to take out my tonsils. I never got it again 😁 (probably coincidence?). I’ve still got them now.
Phew! That was lucky Ukie, I had my out in 1970/71.
Have recently got my nhs old notes. I had lots of tonsilitis, coughs & then prob due to antibiotics each time, uti's each time, just after having 9mnth innoculations as a baby. Seems this settled after few yrs, but ear infections/utis cont.
Just after tetanus jab at 15 I started getting tonsilitis each month again & over those 2 yrs had 20 courses of antibiotics, & plenty moire to follow I'm shocked to read it! Started to get sinusitis too & yes, more uti's!
At 24, 2nd yr of primary teaching & plenty of bugs, came vto a standstill & diagnosed with ME& at 6 1/2 stone, advused to have tonsils removed, then subsequently got sinusitis each month instead!
Can see at that time my ferritinvwas 11, (never even told to take iron) b12 in 200's, same level it was when I've since, many many years on got a functional b12 diagnosis, & thyroid is up & down, currently at 30% through range & trying to question whether it's behind all this, or just affected by other deficiencies!
Have had candida along way, & knowvall those antibiotics and more messed my stomach up.
Still bad sinus issues & due polyps removal.
So yes, think my tonsils were telling me my system was not well, but unfortunately noone could help tell me the real reasons.
It's so frustrating as I was into healthy eating, exercise, etc, but at that age in life believed the Drs were doing right! Turned 50 now and determined to get some better health...
That's my rant over!
Jo that is so similar to myself. I got diagnosed with ME/CFS I have enlarged red blood cells to, which normally means hypoxia at cellular level. Loads of throat and sinus problems. Finely got my notes 15 years later, as as plain as the nose of my face low B12, low thyroid, the whole 9 yards and my doctor never said a thing!
Hi Katherine1234, I'm so sorry I must've show missed replying to this.It's so too frustrating and disappointing for words isn't it! So sorry you experienced similar.
And all these years on, so many Drs still have to have these symptoms and conditions explained to them by desperate patients!
I'd not heard of what you called the large blood cells. I've recently had 3 mnthly bloods & can see mch is still overange, although mcv a bit improved.
I've been reading how lymphocytes can be below range with b12 deficiency and can see tests always been an issue with me too. Interesting guy they came back up.inyo range after loading dose, but now below again.
Hoping you're doing ok...
No problem Jo. Over range of MCV's MCHC's and MCH's mean enlarged red blood cells.
Hi, yes, thanks, I understood they can be enlarged but not heard of the term hypoxia, kearn something new everyday:)I'm not understanding why my mch isn't lowering, 9 months in, aside from it being I'm not having enough b12?
My haemoglobin and rbc lowered considerably over 9mnths of injections, so thought that would've had an effect on lowering the mch as know iron and b12 work against each other in terms of blood cell sizes and can paint a confusing picture!
Tonsils and adenoids out before age two. Major strep infections from SA. So far, Bethesda 6 hobnailed variant papillary thyroid cancer survivor.
<3
Pages 1-2 from the late Dr. Broda Barnes book: Hypothyroidism, the unexpected illness, lists descriptions of the types of patients who passed through his waiting room, on a daily basis, while he was a practicing doctor. I'll paraphrase: A rundown young housewife who is oversensitive to cold weather, a middle-aged man who has become fatigued, a victim of recurrent headaches, a barren couple, "A child or adult unusually prone to infections, particularly respiratory, but not limited to them", etc. He states, "Varied as their symptoms are, the cause of their illness in every case is the same---low thyroid function."
As a child and through my teens, I was sick annually with tonsillitis, strep throat, colds, and URI's.
I just finished watching the 60 mins plus Youtube movie, Earthing Movie. It makes a lot of sense to me to chuck our shoes and ground ourselves to the Earth! I'll try anything at this point. Our Tennessee temperatures have dipped down to the 40'sF and upper 30'sF. I have the winter clothing to keep me warm, and yet I'm freezing. I can't get motivated to do anything, but sit in front of a heater. I want my life back.
I too run low body temperature it is awful and you cannot muster much energy. I also wonder if we are all suffering with a lot of nutritional plus mineral deficits now. I am a great believer in grounding. The native American Indians knew a thing or too about going bare foot and contacting the earth. I also sleep on a grounding sheet at night. Choline and a teaspoon of raw cold pressed coconut oil - 3 times a day put up my body temperature a bit.
I just ordered the small pad for my feet to see if it makes a difference. (Grow my hair back? Stop my Bursitis?) Cease the overall inflammation? Do you see a difference with your sheet?
Conny, my bursitis was caused by low B12, I had it in my hip. Grounding will help. My hair falling out was not being treated properly for thyroid, I am now on T3 as well. I also started taking desiccated liver capsules and copper capsules which stopped it falling out. Anything with itis on the end is inflammation I would get my antioxidant's up big time too.
My hair is still breaking off and on the dry side which means for me low protein, I am going to also take collagen in the new year as our hair, finger nails, joints, muscles, tendons, skin is made up of the stuff. I have low stomach acid after 4 rounds of strong antibiotics, it did my stomach acid and microbiome in. I am having to take HCL, digestive enzymes, and bile salts. When It was really bad I lost the taste for meat and could not digest it. The taste for meat is slowly coming back.
I saw a big difference with my grounding sheet first off, say first couple of months. I really don't see a difference now, it might be I am use to it now, but does not mean it might it has stopped working. I wake up more refreshed now.
My baldness is due to Alopecia, which is genetic in my case. My front hair line has receded to the top of my head and is continuing to recede. I look like Queen Victoria or a character from a Dickens novel. It's awful to see myself smoothly bald as a cue ball on the front half of my head. But it could be worse, right?
I need to wake up refreshed, so I hope that the grounding mat can at least help with that. All of my Hashi/Thyroid/Alopecia issues came with the onset of menopause. Thank you for your reply.
I am so sorry to hear that Have you had your B12 checked?
had tonsils, adenoids out at 4, and appendix removed at 15
I had mine out aged 5 in 1956, but I have Graves disease - overactive thyroid.
I had my tonsils and adenoids out when I was about 6 or 7 years old. I have Hashimoto's diagnosed when I was around 37.
Karen
I suffered from repeated sore throats and asthma throughout my childhood. My tonsils and adenoids were removed at 13 years old. I developed Vitiligo at 15 and I now recognise the first signs of an underactive thyroid at 17. I have several AI conditions. Definitely believe that the tonsillectomy triggered it all.ATVMWF
Wow! That is all autoimmune, how awful have you considered the vitiligo is low B12 and thiamine, low stomach acid causing you not to be able to absorb it? i remember Dr Chandy being very vigilant about this and asking me as l had small teeny patches of it on my forehead and forearms. i was one of those people with not strong enough stomach acid so I was not absorbing my minerals and other nutrients especially b12 and thiamine B1. Low magnesium also has connotations with asthma. You need strong stomach acid to absorb magnesium. I had to resort to magnesium oil spray, sprayed on me and rubbed in, as magnesium absorbs very well through the skin. I really noticed a difference. Some people do magnesium injections into their tummy but it is painful. not for me, I don't do pain very well :/ i self inject B12 into my thigh, no problem there.
I have had continual stomach issues, such as, chronic diverticulitis and hiatus hernia operation. Also early hysterectomy after years and years of gynae problems. Recently a private blood test advised that I ask my GP for an MMA test for low vit B12. My mum had P. A. I chose to supplement myself as GP useless. My whole life has been dogged by ill health and I suspect that I had an issue at birth that was missed. I was only 3llb 4oz at birth and not expected to survive. Baptised in the hospital etc....
I tend to take quite a few supplements and take matters into my own hands after years of gaslighting by the medical profession. It took over 30 years to get diagnosed with thyroid problems for instance, despite numerous tests reporting I was "borderline" and I was having LOTS of subsidiary issues associated with thyroid. Doctors just don't want to see in many cases IMHO.
ATVMWF
I am on the same page as you with regards to gaslighting from the medical profession. The only trouble is when you take B12 supplements it shows high in your blood and they say you are ok even if you may be not absorbing it. This happen to me. It sounds like you will need lots of B12 injections. I had to start off daily with injections for a year! Then went every other day for 2 years. I am now twice a week. Low stomach acid stopped me absorbing most of my vitamins and minerals especially B12. Borderline means you are very low. I would have the MMA and a homocysteine test to check properly regarding B12. I also have enlarged red blood cells which show up on a complete blood panel as high MCV's high MCH, and high MCHV's. A sign of pernicious anemia.
With regards to your hiatus hernia and diverticulitis you could be low on copper which strengthens our soft muscle walls, inside of veins, aorta etc. Brain likes copper and thyroid.. My son had a hiatus hernia, piles, varicose veins, and tummy issues, I gave him copper and everything started to get better. I take quite high dose daily copper, making sure I balance it out with zinc.
It is a journey!
Thanks for all this info, very interesting. I need to reread it tomorrow when I have more time. Can you tell me more about the copper and how/what dosage you recommend. I currently take 75mg T4 and 20 mg T3 daily plus Vit D3 +k2, B12 and Seabuckthorn oil.ATVMWF
That is the same T4 and T3 dose I take. Copper I personally started off with 6 mgs daily for 2 weeks, went up to 9 mgs daily for 2 weeks and I have fixed on 12 mgs daily now for the last 3 months, not sure if I will up it again, I will see how I feel. I take 30 mgs of zinc 3 times a week for the copper/zinc balance. Choline, B5, and MSM natural sulphur crystals have all been a big game changer for me. I take high dose boron for my bones too, then selenium and L Tyrosine for my thyroid. I take high dose K2, 200 daily as I wanted to get plaque off of the back of my lower teeth and don't want calcium plaque in my arteries and other soft tissues, it is working. I do not take D3, I make sure I am in the sun daily for at least 15 minutes spring and summer months. Come December/January/February I take 10 iu's daily and leave it off at weekends. I take potassium as cream of tarter a small teaspoonful chugged down with water when I inject B12, injected B12 takes down my potassium. I also take high dose folate when I inject. I also take daily magnesium, natural vitamin C and a good multi B vit (I rattle). I take others as well as I have also be diagnosed with that nefarious diagnoses of ME/CFS. I self inject b12. get your B12 tests done it is important because the 2 can run hand in hand.
I never had my tonsils out but they gave me an awful lot of bother as a child!
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T3 - I am just wondering as I so often do!
Before you say it, I know I know, I am overthinking!!!!! But arn't we all looking for answers?...
sore burning swollen tonsils and ear and neck pain
I have had sore burning swollen tonsils and ear and neck pain for 4 months and have had multiple...
I am done
EDIT: thank you all so very much for your support, you have no idea how much it means when you are...
Start HC and surgery
I am Hashimotos
Hashi Question?
Hi I am new to Thyroid UK Support, but pleased I have found out about it, as I think I have Hypothyroidism [ I have fibromyalgia ] and am 
